- Chapter 1: Structure and Bonding
- Chapter 10: Alkenes
- Chapter 11: Alkynes
- Chapter 12: Oxidation and Reduction
- Chapter 13: Mass Spectrometry and Infrared Spectroscopy
- Chapter 14: Nuclear Magnetic Resonance Spectroscopy
- Chapter 15: Radical Reactions
- Chapter 16: Conjugation, Resonance, and Dienes
- Chapter 17: Benzene and Aromatic Compounds
- Chapter 18: Electrophilic Aromatic Substitution
- Chapter 19: Carboxylic Acids and the Acidity of the OH Bond
- Chapter 2: Acids and Bases
- Chapter 20: Introduction to Carbonyl Chemistry; Organometallic Reagents; Oxidation and Reduction
- Chapter 21: Aldehydes and KetonesNucleophilic Addition
- Chapter 22: Carboxylic Acids and Their DerivativesNucleophilic Acyl Substitution
- Chapter 23: Substitution Reactions of Carbonyl Compounds at the ` Carbon
- Chapter 24: Carbonyl Condensation Reactions
- Chapter 25: Amines
- Chapter 26: CarbonCarbon Bond-Forming Reactions in Organic Synthesis
- Chapter 27: Carbohydrates
- Chapter 28: Amino Acids and Proteins
- Chapter 29: Lipids
- Chapter 3: Introduction to Organic Molecules and Functional Groups
- Chapter 30: Synthetic Polymers
- Chapter 4: Alkanes
- Chapter 5: Stereochemistry
- Chapter 6: Understanding Organic Reactions
- Chapter 7: Alkyl Halides and Nucleophilic Substitution
- Chapter 8: Alkyl Halides and Elimination Reactions
- Chapter 9: Alcohols, Ethers, and Epoxides
Organic Chemistry 3rd Edition - Solutions by Chapter
Full solutions for Organic Chemistry | 3rd Edition
Any reaction in which an atom or group of atoms is substituted for another atom or group of atoms at an allylic carbon.
Refers to the capacity of a substance to either add or lose a proton 1H+2. (Section 16.2)
An sp3 -hybridized carbon bonded to a benzene ring
A device for measuring the heat evolved in the combustion of a substance under constant-volume conditions. (Section 5.5)
The enthalpy change required to break a bond in a mole of gaseous molecules. (9.10)
Carboxyl group (Section 1.3D)
A !COOH group.
A law stating that at constant pressure, the volume of a given quantity of gas is proportional to absolute temperature. (Section 10.3)
A chemical reaction that proceeds with evolution of heat and usually also a flame; most combustion involves reaction with oxygen, as in the burning of a match. (Section 3.2)
In bond-line structures, agroup going behind the page.
electrospray ionization (ESI):
In mass spectrometry, an ionization technique in which the compound is first dissolved in a solvent and then sprayed via a high-voltage needle into a vacuum chamber. The tiny droplets of solution become charged by the needle, and subsequent evaporation forms gas-phase molecular ions that typically carry one or more charges.
A reaction in which the Gibbs free energy of the products is higher than that of the reactants. The position of equilibrium for an endergonic reaction favors starting materials
A compound containing a hydroxyl group (OH) connected directly to a carbon-carbon double bond.
Lanthanide and actinide elements in which the 4f or 5f orbitals are partially occupied. (Section 6.9)
nonmetallic elements (nonmetals)
Elements in the upper right corner of the periodic table; nonmetals differ from metals in their physical and chemical properties. (Section 2.5)
Any reaction in which one nucleophile is substituted for another at a tetravalent carbon atom.
A form of lipid molecule that contains charged phosphate groups. (Section 24.9)
When electromagnetic radiation is viewed as a particle, an individual packet of energy.
A compound containing several ether groups.
Sigma (s) molecular orbital
A molecular orbital in which electron density is concentrated between two nuclei, along the axis joining them, and is cylindrically symmetrical
In nomenclature, the groups connected to the parent chain.